510(k) K150360
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 4, 2015
- Date Received
- February 12, 2015
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Dilator, Vessel, For Percutaneous Catheterization
- Device Class
- Class II
- Regulation Number
- 870.1310
- Review Panel
- CV
- Submission Type